ClinVar Miner

Variants studied for Paragangliomas 3

Coded as:
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
17 12 11 4 9 53

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
SDHC 16 12 11 4 4 47
SDHD 0 0 0 0 4 4
CFAP126, SDHC 1 0 0 0 0 1
MPZ, SDHC 0 0 0 0 1 1

Submitter and significance breakdown #

Total submitters: 19
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Myriad Genetics, Inc. 14 9 4 1 0 28
Counsyl 0 0 5 3 1 9
Color Diagnostics, LLC DBA Color Health 1 2 2 0 2 7
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 0 7 7
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 1 3 1 0 0 5
OMIM 3 0 0 0 0 3
Center for Human Genetics, Inc, Center for Human Genetics, Inc 3 0 0 0 0 3
Labcorp Genetics (formerly Invitae), Labcorp 1 1 0 0 0 2
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 0 0 1 0 2
Biesecker Lab/Clinical Genomics Section, National Institutes of Health 1 0 0 0 0 1
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia 0 0 0 0 1 1
Institute of Human Genetics, University Hospital of Duesseldorf 1 0 0 0 0 1
Genetics and Molecular Pathology, SA Pathology 0 0 1 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 1 0 0 0 1
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 0 0 1 0 0 1
Department of Medical Genetics, College of Basic Medicine, Army Medical University 1 0 0 0 0 1
New York Genome Center 1 0 0 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 0 1 0 0 1
Gemeinschaftspraxis fuer Humangenetik Dresden 0 1 0 0 0 1

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